K243991
- 510(k) number
- K243991
- Device name
- Klassic Knee System - Revision Tibial Baseplate
- Applicant
- Total Joint Othopedics, Inc. UT · US
- Product code
- JWH — Prosthesis, Knee, Patellofemorotibial, Semi-Constrai
- Decision date
- 2025-03-24
- Date received
- 2024-12-26
- Decision
- Substantially Equivalent
- Clearance type
- Traditional
- Advisory committee
- Orthopedic
510(k) Summary (official FDA PDF): K243991.pdf
Official FDA record: K243991
Data from the openFDA 510(k) dataset (CC0). A 510(k) clearance is not an FDA approval or certification.